Does ECULIZUMAB Cause Device issue? 94 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 94 reports of Device issue have been filed in association with ECULIZUMAB (SOLIRIS). This represents 0.2% of all adverse event reports for ECULIZUMAB.
94
Reports of Device issue with ECULIZUMAB
0.2%
of all ECULIZUMAB reports
2
Deaths
10
Hospitalizations
How Dangerous Is Device issue From ECULIZUMAB?
Of the 94 reports, 2 (2.1%) resulted in death, 10 (10.6%) required hospitalization, and 1 (1.1%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ECULIZUMAB. However, 94 reports have been filed with the FAERS database.
What Other Side Effects Does ECULIZUMAB Cause?
Fatigue (4,858)
Off label use (4,228)
Haemoglobin decreased (3,028)
Headache (2,699)
Death (2,221)
Pyrexia (1,948)
Dyspnoea (1,819)
Asthenia (1,732)
Drug ineffective (1,644)
Nausea (1,579)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ECULIZUMAB Alternatives Have Lower Device issue Risk?
ECULIZUMAB vs EDARAVONE
ECULIZUMAB vs EDETATE
ECULIZUMAB vs EDOXABAN
ECULIZUMAB vs EDOXABAN TOSILATE
ECULIZUMAB vs EFALIZUMAB